Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure

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Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.MPV17-related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects.

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Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 July 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Incidence of Primary Mitochond ...... nting With Acute Liver Failure

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Incidence of Primary Mitochond ...... ting With Acute Liver Failure.

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Incidence of Primary Mitochond ...... nting With Acute Liver Failure

@en

Incidence of Primary Mitochond ...... ting With Acute Liver Failure.

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Incidence of Primary Mitochond ...... nting With Acute Liver Failure

@en

Incidence of Primary Mitochond ...... ting With Acute Liver Failure.

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Incidence of Primary Mitochond ...... nting With Acute Liver Failure

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Carl Fratter

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Girish Gupte

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Iain Hargreaves

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Kate Craig

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Katherine Foster

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Khalid Sharif

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Patrick McKiernan

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Robert W Taylor

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Sarah Ball

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Shamima Rahman

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P2860

Clinical and molecular features of mitochondrial DNA depletion syndromes.

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy.

Etiology, outcome and prognostic indicators of childhood fulminant hepatic failure in the United kingdom.

Mitochondrial DNA and disease.

Reduced mitochondrial DNA content and heterozygous nuclear gene mutations in patients with acute liver failure.

Evaluation of the child with suspected mitochondrial liver disease

Acute infantile liver failure due to mutations in the TRMU gene.

Gastrointestinal and hepatic manifestations of mitochondrial disorders.

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592-597

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scholarly article

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10.1097/MPG.0000000000001345

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English

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Robert McFarland

Joanna Poulton

Saikat Santra

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2016-12-01T00:00:00Z

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27482763

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5113754

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Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure

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P2860

P2860

Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932